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Polysiloxanes polymers

SPh determination of silicon and phosphorus in form of Si-Mo and P-Mo heteropolyacids are used successfully for series determination of these heteroelements in OEC and polymers (polysiloxanes, polyphosphazenes, etc.). [Pg.187]

Surface chemistry and thermodynamics, Surface Tension Surfactants. Defoamers, antifoams, anti flood and float, wetting aids, emulsifiers, levelling agents, pigment dispersants. Colorant acceptor Water repellents. Numerous aniottic, non-ioruc, cationic and an hoteric agents. Silicones an hipafhic polymers. Polysiloxanes... [Pg.39]

Polyphenylene sulfide, see High-temperature polymers Polysiloxane... [Pg.1429]

This section cited some interesting polyviologens and reported a two-step synthesis by which two classes of polymers, polysiloxanes, and polyviologens are combined to produce a hybrid copolymer. The synthesis of an AB2-type monomer from TMDS and a vinyl monomer was achieved at room temperature. The first step of the reaction is quantitative and time dependent. The hybrid copolymer is characterized by FT-IR and H-NMR spectroscopy. The siloxane-based polymer without the Si-O-C bond is thermally stable. Applications of the hybrid copolymer are expected in the packaging and food industries and as a new biocidal material. [Pg.182]

Silicone polymers (polysiloxanes) form a group of materials of unusual properties which may include high-thermal stabilities, low-surface energies and low values. Not surprisingly there has... [Pg.1157]

Cased W, Sauer T and Wegner G 1988 Soluble phthalocyaninato-polysiloxanes—rigid rod polymers of high molecular-weight/Macromo/. Chem. Rapid Commun. 9 651-7... [Pg.2634]

Gyclodextrins. As indicated previously, the native cyclodextrins, which are thermally stable, have been used extensively in Hquid chromatographic chiral separations, but their utihty in gc appHcations was hampered because their highly crystallinity and insolubiUty in most organic solvents made them difficult to formulate into a gc stationary phase. However, some functionali2ed cyclodextrins form viscous oils suitable for gc stationary-phase coatings and have been used either neat or diluted in a polysiloxane polymer as chiral stationary phases for gc (119). Some of the derivati2ed cyclodextrins which have been adapted to gc phases are 3-0-acetyl-2,6-di-0-pentyl, 3-0-butyryl-2,6-di-0-pentyl,... [Pg.70]

Fig. 2. Molecular structures of selected photoconductive polymers with pendent groups (1) poly(A/-vinylcarba2ole) [25067-59-8] (PVK), (2) A/-polysiloxane carbazole, (3) bisphenol A polycarbonate [24936-68-3] (4) polystyrene [9003-53-6] (5) polyvin5i(l,2-/n7 j -bis(9H-carba2ol-9-yl)cyclobutane) [80218-52-6]... Fig. 2. Molecular structures of selected photoconductive polymers with pendent groups (1) poly(A/-vinylcarba2ole) [25067-59-8] (PVK), (2) A/-polysiloxane carbazole, (3) bisphenol A polycarbonate [24936-68-3] (4) polystyrene [9003-53-6] (5) polyvin5i(l,2-/n7 j -bis(9H-carba2ol-9-yl)cyclobutane) [80218-52-6]...
Maxillofacial polymers include the chlorinated polyethylenes, polyethemrethanes, polysiloxanes (see Elastomers), and conventional acrylic polymers. These are all deficient in a number of critical performance and processing characteristics. It is generally agreed that there is a need for improved maxillofacial polymers that can be conveniently fabricated into a variety of prostheses (218,227,228). [Pg.490]

Syltheiin XLT (Dow Corning Coiporation). A sihcone polymer (Dimethyl Polysiloxane) recommended temperature range —70°C to 250°C odorless low in acute oral toxicity noncorrosive toward metals and alloys commonly found in heat transfer systems,... [Pg.1125]

Stmctural and chemical modification of urethane containing polymer matri-ces with macrocycles - calixarenes having reactive hydrazide groups have been carried out and stmcture, physico chemical and sensor properties of polyure-thanesemicarbazides (PUS) synthesised have been studied. The polymers obtained (on the base of polypropylene glycol MM 1000 and polysiloxane diol MM 860, hexamethylene diisocyanate and calixarene dihydrazide) are identified by IR-spectroscopy, size exclusion chromatography (SEC), DSC, WAXS and SAXS methods. [Pg.327]

A new brush-type CSP, the Whelk-0 1, was used by Blum et al. for the analytical and preparative-scale separations of racemic pharmaceutical compounds, including verapamil and ketoprofen. A comparison of LC and SFC revealed the superiority of SFC in terms of efficiency and speed of method development [50]. The Whelk-0 1 selector and its homologues have also been incorporated into polysiloxanes. The resulting polymers were coated on silica and thermally immobilized. Higher efficiencies were observed when these CSPs were used with sub- and supercritical fluids as eluents, and a greater number of compounds were resolved in SFC compared to LC. Compounds such as flurbiprofen, warfarin, and benzoin were enantioresolved with a modified CO, eluent [37]. [Pg.307]

As an organic polymer, poly(tetramethylene oxide) was also used for the preparation of ceramers. The mechanical properties in these cases were much improved in comparison with those for hybrids from polysiloxanes. In these poly (tetramethylene oxide)-silica hybrids, the effect of the number of functional triethoxysilyl groups was examined [13]. As shown in Fig. 2, more multifunctional organic polymer produced more crosslinked hybrid networks. This means that the more rigid the structure in the hybrids is, the higher the modulus and the lower swelling property. [Pg.15]

In summary, silica gel can be an excellent stationary phase for use in exclusion chromatography in the separation of high molecular weight, weakly polar or polarizable polymers. It cannot be used for separating mixtures that require an aqueous mobile phase or operate at a pH outside the range of 4-8. Examples of the type of materials that can be separated by exclusion chromatography using silica gel are the polystyrenes, polynuclear aromatics, polysiloxanes and similar polymeric mixtures that are soluble and stable in solvents such as tetrahydrofuran. [Pg.71]


See other pages where Polysiloxanes polymers is mentioned: [Pg.193]    [Pg.182]    [Pg.474]    [Pg.18]    [Pg.25]    [Pg.55]    [Pg.287]    [Pg.22]    [Pg.862]    [Pg.466]    [Pg.175]    [Pg.369]    [Pg.193]    [Pg.182]    [Pg.474]    [Pg.18]    [Pg.25]    [Pg.55]    [Pg.287]    [Pg.22]    [Pg.862]    [Pg.466]    [Pg.175]    [Pg.369]    [Pg.70]    [Pg.332]    [Pg.47]    [Pg.63]    [Pg.242]    [Pg.12]    [Pg.509]    [Pg.678]    [Pg.680]    [Pg.686]    [Pg.435]    [Pg.3]    [Pg.15]    [Pg.4]    [Pg.6]    [Pg.33]    [Pg.11]    [Pg.23]    [Pg.37]    [Pg.40]    [Pg.41]    [Pg.43]    [Pg.48]   
See also in sourсe #XX -- [ Pg.113 , Pg.362 , Pg.380 ]




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High-temperature polymer polysiloxane

Linear polysiloxanes polymers

Phthalocyaninato polysiloxane polymer

Polymer processing polysiloxane polymers

Polymer reaction polysiloxane

Polymers/Polymerization polysiloxane

Polysiloxane

Polysiloxane liquid crystal polymers

Polysiloxane polymers

Polysiloxane polymers

Polysiloxanes

Polysiloxanes and Related Polymers

Side-chain liquid crystalline polymers polysiloxane

Silicon-Oxygen Polymers Polysiloxanes (Silicones)

Siloxane polymers Polysiloxanes

Substituted polysiloxane polymers

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